Canonical Allele Identifier: PA2825750567
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 285159
ClinVar RCV Id: RCV000725599 RCV001495704
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Gly1460Ser
CA1707026
NM_001130977.2:c.4378G>A